Taiwan FDA registration 6436b0baccb95bb66039306d680a6237
"Bidi" blood return vacuum blood collection needle
TW: "必帝" 回血式真空採血針
Taiwan·Risk Class 2·BECTON DICKINSON MEDICAL(S) PTE. LTD.·Registered Oct 26, 2004 – Oct 26, 2029ActiveRegistration details
- Analysis ID
- 6436b0baccb95bb66039306d680a6237
- Customs Code
- DHA00601089101
Company information
- Manufacturer
- BECTON DICKINSON MEDICAL(S) PTE. LTD.
- Manufacturer Country
- Singapore
- Authorized Representative
- BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- import
Dates and status
- Registration Date
- Oct 26, 2004
- Expiry Date
- Oct 26, 2029
About this record
Access comprehensive regulatory information for "Bidi" blood return vacuum blood collection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6436b0baccb95bb66039306d680a6237 and manufactured by BECTON DICKINSON MEDICAL(S) PTE. LTD.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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